Linked Data
MyVariant Identifiers:
chr3:g.14180730G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.14139230G>C , CM000665.2:g.14139230G>C | GRCh38 |
| NC_000003.11:g.14180730G>C , CM000665.1:g.14180730G>C | GRCh37 |
| NC_000003.10:g.14155731G>C | NCBI36 |
| NG_008975.1:g.19291G>C , LRG_435:g.19291G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000432444.2:c.*963G>C | ENSP00000395617.1:n.*963G>C | |
| ENST00000306077.5:c.933G>C MANE Select | ENSP00000303992.5:p.Leu311= | |
| ENST00000306077.4:c.933G>C | ENSP00000303992.4:p.Leu311= | |
| ENST00000601399.3:n.260G>C | ||
| ENST00000608606.1:c.169G>C | ||
| NM_024334.2:c.933G>C , LRG_435t1:c.933G>C | NP_077310.1:p.Leu311= | |
| XM_011534109.1:c.828G>C | XP_011532411.1:p.Leu276= | |
| XM_017007176.2:c.828G>C | XP_016862665.1:p.Leu276= | |
| NM_024334.3:c.933G>C MANE Select | NP_077310.1:p.Leu311= |